Late-stage (radio)fluorination of alkyl phosphonates via electrophilic activation
Constructing organic fluorophosphines, vital drug skeletons, through the direct fluorination of readily available alkyl phosphonates has been impeded due to the intrinsic low electrophilicity of PV and the high bond energy of P═O bond.
Kaiqiang Zhang +8 more
doaj +1 more source
Rapid, efficient, and economical synthesis of PET tracers in a droplet microreactor: application to O-(2-[18F]fluoroethyl)-L-tyrosine ([18F]FET). [PDF]
BackgroundConventional scale production of small batches of PET tracers (e.g. for preclinical imaging) is an inefficient use of resources. Using O-(2-[18F]fluoroethyl)-L-tyrosine ([18F]FET), we demonstrate that simple microvolume radiosynthesis ...
Chen, Bao Ying +5 more
core +1 more source
Background Infections pose a significant risk to immunocompromised individuals, and accurate, efficient diagnosis remain challenging. Current imaging methods like MRI and FDG PET lack pathogen specificity which complicate diagnosis and lead to overuse of
Amy L. Vāvere +6 more
doaj +1 more source
Nukleophile Kupfer-Vermittelte Radiofluorierung von L-Tryptophan-Derivaten [PDF]
$^{18}$F-Labeled aromatic amino acids became more and more important for molecular imgaging withPositron Emission Tomography (PET). Several examples have emerged showing higherspecificity in imaging disorders in neurological processes or tumors.
Schäfer, Dominique Christian
core
Peptides Radiofluorination: Main Methods and Highlights
Ana Carolina A. Bispo +3 more
openaire +1 more source
Background (S)-[18F]FETrp is a promising PET radiotracer for imaging IDO1 activity, one of the main enzymes involved in the tryptophan metabolism that plays a key role in several diseases including cancers.
Aurélie Maisonial-Besset +6 more
doaj +1 more source
Automated synthesis and PET evaluation of both enantiomers of [18F]FMISO [PDF]
Hansen, Anders Elias +6 more
core +1 more source
Synthesis and radiofluorination of putative NMDA receptor ligands
In the course of this work on the synthesis of radioligands for the NMDA receptor the authentic standards and labeling precursors of four compounds with an amidine structure was performed. Synthesis of the precursors followed reaction conditions given in the literature and was successful.
openaire +3 more sources
On the Risk of <sup>18</sup>F-Regioisomer Formation in the Copper-Free Radiofluorination of Aryliodonium Precursors. [PDF]
Zhao Q +4 more
europepmc +1 more source
Streamlined Radiosynthesis of [18F]Fluproxadine (AF78): An Unprotected Guanidine Precursor Enables Efficient One-Step, Automation-Ready Labeling for Clinical Use. [PDF]
Chen X +9 more
europepmc +1 more source

